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Reduced P2X receptor levels are associated with antidepressant effect in the learned helplessness model
Purinergic receptors, especially P2RX, are associated to the severity of symptoms in patients suffering from depressive and bipolar disorders, and genetic deletion or pharmacological blockade of P2RX7 induces antidepressant-like effect in preclinical models. However, there is scarce evidence about t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812674/ https://www.ncbi.nlm.nih.gov/pubmed/31656696 http://dx.doi.org/10.7717/peerj.7834 |
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author | Ribeiro, Deidiane Elisa Casarotto, Plinio C. Staquini, Laura Pinto e Silva, Maria Augusta Biojone, Caroline Wegener, Gregers Joca, Samia |
author_facet | Ribeiro, Deidiane Elisa Casarotto, Plinio C. Staquini, Laura Pinto e Silva, Maria Augusta Biojone, Caroline Wegener, Gregers Joca, Samia |
author_sort | Ribeiro, Deidiane Elisa |
collection | PubMed |
description | Purinergic receptors, especially P2RX, are associated to the severity of symptoms in patients suffering from depressive and bipolar disorders, and genetic deletion or pharmacological blockade of P2RX7 induces antidepressant-like effect in preclinical models. However, there is scarce evidence about the alterations in P2RX7 or P2RX4 levels and in behavioral consequences induced by previous exposure to stress, a major risk factor for depression in humans. In the present study, we evaluated the effect of imipramine (IMI) on P2RX7 and P2RX4 levels in dorsal and ventral hippocampus as well as in the frontal cortex of rats submitted to the pretest session of learned helplessness (LH) paradigm. Repeated, but not acute administration of IMI (15 mg/kg ip) reduced the levels of both P2RX7 and P2RX4 in the ventral, but not in dorsal hippocampus or frontal cortex. In addition, we tested the effect of P2RX7/P2RX4 antagonist brilliant blue G (BBG: 25 or 50 mg/kg ip) on the LH paradigm. We observed that repeated (7 days) but not acute (1 day) treatment with BBG (50 mg) reduced the number of failures to escape the shocks in the test session, a parameter mimicked by the same regimen of IMI treatment. Taken together, our data indicates that pharmacological blockade or decrease in the expression of P2RX7 is associated to the antidepressant-like behavior observed in the LH paradigm after repeated drug administration. |
format | Online Article Text |
id | pubmed-6812674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68126742019-10-25 Reduced P2X receptor levels are associated with antidepressant effect in the learned helplessness model Ribeiro, Deidiane Elisa Casarotto, Plinio C. Staquini, Laura Pinto e Silva, Maria Augusta Biojone, Caroline Wegener, Gregers Joca, Samia PeerJ Animal Behavior Purinergic receptors, especially P2RX, are associated to the severity of symptoms in patients suffering from depressive and bipolar disorders, and genetic deletion or pharmacological blockade of P2RX7 induces antidepressant-like effect in preclinical models. However, there is scarce evidence about the alterations in P2RX7 or P2RX4 levels and in behavioral consequences induced by previous exposure to stress, a major risk factor for depression in humans. In the present study, we evaluated the effect of imipramine (IMI) on P2RX7 and P2RX4 levels in dorsal and ventral hippocampus as well as in the frontal cortex of rats submitted to the pretest session of learned helplessness (LH) paradigm. Repeated, but not acute administration of IMI (15 mg/kg ip) reduced the levels of both P2RX7 and P2RX4 in the ventral, but not in dorsal hippocampus or frontal cortex. In addition, we tested the effect of P2RX7/P2RX4 antagonist brilliant blue G (BBG: 25 or 50 mg/kg ip) on the LH paradigm. We observed that repeated (7 days) but not acute (1 day) treatment with BBG (50 mg) reduced the number of failures to escape the shocks in the test session, a parameter mimicked by the same regimen of IMI treatment. Taken together, our data indicates that pharmacological blockade or decrease in the expression of P2RX7 is associated to the antidepressant-like behavior observed in the LH paradigm after repeated drug administration. PeerJ Inc. 2019-10-21 /pmc/articles/PMC6812674/ /pubmed/31656696 http://dx.doi.org/10.7717/peerj.7834 Text en © 2019 Ribeiro et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Animal Behavior Ribeiro, Deidiane Elisa Casarotto, Plinio C. Staquini, Laura Pinto e Silva, Maria Augusta Biojone, Caroline Wegener, Gregers Joca, Samia Reduced P2X receptor levels are associated with antidepressant effect in the learned helplessness model |
title | Reduced P2X receptor levels are associated with antidepressant effect in the learned helplessness model |
title_full | Reduced P2X receptor levels are associated with antidepressant effect in the learned helplessness model |
title_fullStr | Reduced P2X receptor levels are associated with antidepressant effect in the learned helplessness model |
title_full_unstemmed | Reduced P2X receptor levels are associated with antidepressant effect in the learned helplessness model |
title_short | Reduced P2X receptor levels are associated with antidepressant effect in the learned helplessness model |
title_sort | reduced p2x receptor levels are associated with antidepressant effect in the learned helplessness model |
topic | Animal Behavior |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812674/ https://www.ncbi.nlm.nih.gov/pubmed/31656696 http://dx.doi.org/10.7717/peerj.7834 |
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